Is ghrelin a biomarker of early-onset scoliosis in children with Prader–Willi syndrome?

被引：0

作者：

Dibia Liz Pacoricona Alfaro

Gwenaelle Diene

Graziella Pinto

Jean-Pierre Salles

Isabelle Gennero

Sandy Faye

Catherine Molinas

Marion Valette

Catherine Arnaud

Maithé Tauber

机构：

[1] Inserm - Paul Sabatier University,CERPOP, Toulouse University

[2] Children’s Hospital,Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit

[3] University Hospital Center of Toulouse,French National Reference Center for Prader

[4] University Hospital Center of Toulouse,Willi Syndrome, Children’s Hospital

[5] Necker-Enfants Malades Hospital,Pediatric Endocrinology, Diabetology and Gynecology Department, Assistance

[6] University Toulouse III,Publique Hôpitaux de Paris (AP

[7] University Hospital Center of Toulouse,HP)

[8] University Hospital Center of Toulouse,Toulouse Institute of Infectious and Inflammatory Diseases (Infinity), Inserm UMR1291

[9] Children’s Hospital, CNRS UMR5051

[10] University Hospital Center of Toulouse,French National Reference Center for Rare Diseases of Calcium and Phosphate Metabolism

[11] University Hospital Center of Toulouse, ERN BOND

来源：

Orphanet Journal of Rare Diseases | / 16卷

关键词：

Prader–Willi syndrome; Early-onset scoliosis; Total ghrelin; Acylated ghrelin; Unacylated ghrelin; AG/UAG ratio;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

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